Canonical Allele Identifier: CA374264965
Gene: ALDOB HGNC NCBI

Linked Data

ClinVar Variation Id: 473
ClinVar RCV Id: RCV000000502
dbSNP Id: rs1564077542
MyVariant Identifiers: chr9:g.104187910C>T (hg19) chr9:g.101425628C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101425628C>T , CM000671.2:g.101425628C>T GRCh38
NC_000009.11:g.104187910C>T , CM000671.1:g.104187910C>T GRCh37
NC_000009.10:g.103227731C>T NCBI36
NG_012387.1:g.15153G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647789.2:c.625-1G>A MANE Select ENSP00000497767.1:n.625-1G>A
ENST00000648064.1:c.625-1G>A ENSP00000497990.1:n.625-1G>A
ENST00000648758.1:c.625-1G>A ENSP00000497731.1:n.625-1G>A
ENST00000649902.1:c.625-1G>A ENSP00000497216.1:n.625-1G>A
ENST00000374855.8:c.625-1G>A ENSP00000363988.4:n.625-1G>A
ENST00000468981.3:n.152-1G>A
ENST00000616752.1:c.625-1G>A ENSP00000481363.1:n.625-1G>A
NM_000035.3:c.625-1G>A NP_000026.2:n.625-1G>A
NM_000035.4:c.625-1G>A MANE Select NP_000026.2:n.625-1G>A
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